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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598722Generated: October 30, 2026

Methyl iodide → 1-Chloro-5-(1,1-dimethylethyl)-2-methoxy-3-nitrobenzene

https://huagongshe.com/reaction/598722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant4-tert-Butyl-2-chloro-6-nitrophenolHCID 26749—
SolventAcetoneHCID 180—
Product1-Chloro-5-(1,1-dimethylethyl)-2-methoxy-3-nitrobenzeneHCID 57418548—

Reaction Conditions

Temperature65 °C

Reaction Steps

4-tert-Butyl-2-chloro-6-nitro-phenol (0.214 g, 0.934 mmol) was dissolved in 3 mL acetone and K2CO3 (0.65 g, 4.7 mmol) and MeI (0.58 mL, 9.3 mmol) were added. The reaction was stirred at 65° C. overnight, after which the solvent was removed under reduced pressure. The residue was taken up in DCM, the organic layer was washed with water, dried over MgSO4 and concentrated to yield 0.15 g of target product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897599B2
Source datasetuspto-grants-2011_03
ORD IDord-34477705ab9d4c99a2b494090f106b4c
Source noteuspto-grants-2011_03